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Investigation of Stilbenoids as Potential Therapeutic Agents for Rotavirus Gastroenteritis
Rotavirus (RV) infections cause severe diarrhea in infants and young children worldwide. Vaccines are available but cost prohibitive for many countries and only reduce severe symptoms. Vaccinated infants continue to shed infectious particles, and studies show decreased efficacy of the RV vaccines in...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563088/ https://www.ncbi.nlm.nih.gov/pubmed/26379708 http://dx.doi.org/10.1155/2015/293524 |
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author | Ball, Judith M. Medina-Bolivar, Fabricio Defrates, Katelyn Hambleton, Emily Hurlburt, Megan E. Fang, Lingling Yang, Tianhong Nopo-Olazabal, Luis Atwill, Richard L. Ghai, Pooja Parr, Rebecca D. |
author_facet | Ball, Judith M. Medina-Bolivar, Fabricio Defrates, Katelyn Hambleton, Emily Hurlburt, Megan E. Fang, Lingling Yang, Tianhong Nopo-Olazabal, Luis Atwill, Richard L. Ghai, Pooja Parr, Rebecca D. |
author_sort | Ball, Judith M. |
collection | PubMed |
description | Rotavirus (RV) infections cause severe diarrhea in infants and young children worldwide. Vaccines are available but cost prohibitive for many countries and only reduce severe symptoms. Vaccinated infants continue to shed infectious particles, and studies show decreased efficacy of the RV vaccines in tropical and subtropical countries where they are needed most. Continuing surveillance for new RV strains, assessment of vaccine efficacy, and development of cost effective antiviral drugs remain an important aspect of RV studies. This study was to determine the efficacy of antioxidant and anti-inflammatory stilbenoids to inhibit RV replication. Peanut (A. hypogaea) hairy root cultures were induced to produce stilbenoids, which were purified by high performance countercurrent chromatography (HPCCC) and analyzed by HPLC. HT29.f8 cells were infected with RV in the presence stilbenoids. Cell viability counts showed no cytotoxic effects on HT29.f8 cells. Viral infectivity titers were calculated and comparatively assessed to determine the effects of stilbenoid treatments. Two stilbenoids, trans-arachidin-1 and trans-arachidin-3, show a significant decrease in RV infectivity titers. Western blot analyses performed on the infected cell lysates complemented the infectivity titrations and indicated a significant decrease in viral replication. These studies show the therapeutic potential of the stilbenoids against RV replication. |
format | Online Article Text |
id | pubmed-4563088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-45630882015-09-16 Investigation of Stilbenoids as Potential Therapeutic Agents for Rotavirus Gastroenteritis Ball, Judith M. Medina-Bolivar, Fabricio Defrates, Katelyn Hambleton, Emily Hurlburt, Megan E. Fang, Lingling Yang, Tianhong Nopo-Olazabal, Luis Atwill, Richard L. Ghai, Pooja Parr, Rebecca D. Adv Virol Research Article Rotavirus (RV) infections cause severe diarrhea in infants and young children worldwide. Vaccines are available but cost prohibitive for many countries and only reduce severe symptoms. Vaccinated infants continue to shed infectious particles, and studies show decreased efficacy of the RV vaccines in tropical and subtropical countries where they are needed most. Continuing surveillance for new RV strains, assessment of vaccine efficacy, and development of cost effective antiviral drugs remain an important aspect of RV studies. This study was to determine the efficacy of antioxidant and anti-inflammatory stilbenoids to inhibit RV replication. Peanut (A. hypogaea) hairy root cultures were induced to produce stilbenoids, which were purified by high performance countercurrent chromatography (HPCCC) and analyzed by HPLC. HT29.f8 cells were infected with RV in the presence stilbenoids. Cell viability counts showed no cytotoxic effects on HT29.f8 cells. Viral infectivity titers were calculated and comparatively assessed to determine the effects of stilbenoid treatments. Two stilbenoids, trans-arachidin-1 and trans-arachidin-3, show a significant decrease in RV infectivity titers. Western blot analyses performed on the infected cell lysates complemented the infectivity titrations and indicated a significant decrease in viral replication. These studies show the therapeutic potential of the stilbenoids against RV replication. Hindawi Publishing Corporation 2015 2015-08-26 /pmc/articles/PMC4563088/ /pubmed/26379708 http://dx.doi.org/10.1155/2015/293524 Text en Copyright © 2015 Judith M. Ball et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Ball, Judith M. Medina-Bolivar, Fabricio Defrates, Katelyn Hambleton, Emily Hurlburt, Megan E. Fang, Lingling Yang, Tianhong Nopo-Olazabal, Luis Atwill, Richard L. Ghai, Pooja Parr, Rebecca D. Investigation of Stilbenoids as Potential Therapeutic Agents for Rotavirus Gastroenteritis |
title | Investigation of Stilbenoids as Potential Therapeutic Agents for Rotavirus Gastroenteritis |
title_full | Investigation of Stilbenoids as Potential Therapeutic Agents for Rotavirus Gastroenteritis |
title_fullStr | Investigation of Stilbenoids as Potential Therapeutic Agents for Rotavirus Gastroenteritis |
title_full_unstemmed | Investigation of Stilbenoids as Potential Therapeutic Agents for Rotavirus Gastroenteritis |
title_short | Investigation of Stilbenoids as Potential Therapeutic Agents for Rotavirus Gastroenteritis |
title_sort | investigation of stilbenoids as potential therapeutic agents for rotavirus gastroenteritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563088/ https://www.ncbi.nlm.nih.gov/pubmed/26379708 http://dx.doi.org/10.1155/2015/293524 |
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